Background: Congenital pulmonary stenosis (PS) is a progressive disease. Balloon pulmonary valvuloplasty (BPV) is the treatment of choice in valvular PS.
Aim:We aim to study the relationship between biomarkers and echocardiographic markers in valvular PS and to assess the impact of BPV on these markers.Patients and Methods: Patients with moderate and severe valvular PS amenable for BPV were recruited. Serum troponin I was measured. Echocardiographic assessment of PS and right ventricular (RV) function was done. All patients underwent BPV.Troponin level and echocardiographic data were re-assessed 2 weeks and 6 months after BPV.Results: Fifty patients with valvular PS were recruited. There was significant correlation between peak SPG and troponin (P < .001). Troponin was significantly decreased 2 weeks after BPV. Similarly, there was an initial improvement in RV function. After 6 months of follow-up, we divided patients into two groups: Group A: 36 patients with no restenosis. Group B: 14 patients with restenosis. There were high significant differences between both groups regarding troponin level and RV functions with reelevated troponin in Group B that correlated with peak PG (r = .9, P < .001). RV function parameters in Group B became significantly worse 6 months after BPV than those after the initial 2 weeks.
Conclusion:Troponin correlates with the severity of PS and associates with RV dysfunction. Both troponin and RV functions improved with BPV. Recurrent elevation of troponin and impairment of RV function is associated with PV restenosis and could be set as an indication for repeated balloon dilatation of PV.
Background: Congenital pulmonary stenosis (PS) is a progressive disease.
Balloon pulmonary valvuloplasty (BPV) is the treatment of choice in
valvular PS. Aim: We aim to study the relationship between biomarkers
and echocardiographic markers in valvular PS and to assess the impact of
BPV on these markers. Patients & Methods Patients with moderate and
severe valvular PS amenable for BPV were recruited. Serum troponin I was
measured. Echocardiographic assessment of PS and right ventricular
(RV)function were done. All patients underwent BPV. Troponin level and
echocardiographic data were re-assessed two weeks & six months after
BPV. Results: Fifty patients with valvular PS were recruited. There was
significant correlation between peak SPG and troponin (p <
0.001). Troponin was significantly decreased 2 weeks after BPV.
Similarly, there was an initial improvement in RV function. After 6
months of follow up, we divided patients into 2 groups: Group-A: 36
patients with no restenosis. Group-B: 14 patients with restenosis. There
were high significant differences between both groups regarding troponin
level and RV functions with re-elevated troponin in group-B that
correlated with peak PG (r= 0.9, p < 0.001). RV function
parameters in group-B became significantly worse 6 months after BPV than
those after the initial 2 weeks. Conclusion Troponin correlates with the
severity of PS and associates with RV dysfunction. Both troponin & RV
functions improved with BPV. Recurrent elevation of troponin and
impairment of RV function are associated with PV restenosis and could be
set as an indication for repeated balloon dilatation of PV.
Background: Terminal QRS distortion and fragmentation (fQRS) with elevated myeloperoxidase (MPO) were linked to poor cardiovascular outcomes in acute coronary syndrome. We aimed to investigate these parameters in early prediction of coronary artery disease severity based on SYNTAX score and in-hospital adverse events in STEMI patients. Methods: A total of 215 patients with first STEMI admitted for primary PCI were included in the study. They were divided according to the admission ECG into group I with QRS distortion or fQRS, group II with combined QRS distortion and fQRS, and group III without QRS distortion or fQRS. Myeloperoxidase and troponin I levels, ST resolution ratio, left ventricular EF%, and severity of coronary artery lesions using SYNTAX risk score were measured. Results: MPO level, SYNTAX score, and in-hospital mortality were higher in group I and II and were higher in group II compared to group I. By regression analysis, QRS distortion, fQRS, and MPO > 412 ng/ml were independent predictors of both CAD severity and in-hospital mortality. DM was an independent predictor of CAD severity (OR: 2.851, P 0.012) while high SYNTAX score was an independent predictor of in-hospital mortality (OR: 6.113, P 0.001). Adding MPO level to any QRS configuration pattern increased predictive value for the detection of CAD severity that was more evident in the combined QRS distortion and fragmentation. Conclusion: Terminal QRS distortion, fragmentation, or combined QRS distortion and fragmentation have a significant value in predicting in-hospital adverse events and CAD severity as assessed by SYNTAX score in association with plasma myeloperoxidase level in STEMI patients. Combined QRS distortion and fragmentation, in spite less common, could be more helpful for early risk stratification and management.
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